Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs200922190
CDC73
1.000 0.040 1 193234361 intron variant -/ATAATT delins 0.16 1
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs71361504
BRCA1 ; NBR2
0.925 0.120 17 43125988 intron variant -/GTT delins 2
rs3783553
IL1A
0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs61764370
KRAS
0.662 0.320 12 25207290 3 prime UTR variant A/C snv 6.2E-02 29
rs7201
MMP2
0.925 0.160 16 55505702 3 prime UTR variant A/C snv 0.37 4
rs7041895 1.000 0.040 9 22162795 intergenic variant A/C snv 0.47 3
rs10859871 1.000 0.040 12 95318100 intron variant A/C snv 0.37 2
rs1750034
SYNJ2
1.000 0.040 6 158059112 intron variant A/C snv 0.88 1
rs6546324
LOC105374786
1.000 0.040 2 67629358 intron variant A/C snv 0.71 1
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 12
rs756384853
CD44
1.000 0.040 11 35229167 missense variant A/C;G snv 4.0E-06; 4.0E-06 1
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs10953316
MUC17
1.000 0.040 7 101038481 synonymous variant A/C;G;T snv 8.0E-06; 0.64 1
rs699947
VEGFA
0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs2237895
KCNQ1
0.790 0.240 11 2835964 intron variant A/C;T snv 10
rs3756712
PDCD6 ; AHRR
0.790 0.160 5 308981 non coding transcript exon variant A/C;T snv 10
rs4980524
STIP1
0.882 0.080 11 64191787 intron variant A/C;T snv 3
rs625879
BHMT2 ; DMGDH
0.925 0.080 5 79085866 intron variant A/C;T snv 0.52 2
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs17576
MMP9
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73